BRICKELL Daily Defense Face Moisturizer SPF-20

UNIISPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerBRICKELL BRANDS LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8224722500
59 mL in 1 JAR (82247-225-00)

Annotations

UNII (FDA Substance ID)

4X49Y0596W

OCTISALATE

RxCUI 91327

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "4X49Y0596W",
    "rxcui": "91327",
    "inchikey": "FMRHJJZUHUTGKE-UHFFFAOYSA-N",
    "display_name": "OCTISALATE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "7ba3b13b-cb78-4df8-8719-c88e556643b4": {
      "match": "brand_token",
      "title": "BRICKELL MENS PRODUCTS RELIEVING ANTI-DANDRUFF (SALICYLIC ACID) LIQUID [BRICKELL BRANDS LLC]",
      "spl_version": "1",
      "published_date": "2025-06-17"
    }
  },
  "productid": "82247-225_09e2e2ce-d869-0711-e063-6294a90a9213",
  "productndc": "82247-225",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "OCTISALATE; ZINC OXIDE",
  "proprietary_name": "BRICKELL Daily Defense Face Moisturizer SPF-20",
  "active_ingred_unit": "mg/mL; mg/mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "OCTISALATE, ZINC OXIDE",
  "start_marketing_date": "20210921",
  "active_numerator_strength": "50; 40"
}

Access this data programmatically

Query BRICKELL Daily Defense Face Moisturizer SPF-20 and 610,000+ other drug records through a single REST API — with a last_synced_at provenance stamp on every response. Free tier includes 100 requests/day.

Get a free API key Read the API docs